Allele Registry

Canonical Allele Identifier: PA113062

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015491

ClinVar Variation:

14410

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Leu502Pro	CA250650 NM_000233.4:c.1505T>C